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Thionyl Chloride → HCID 20485210、化合物

HRID 647548
ノート
印刷プレビュー

反応式

HRID 647548 の反応式
[Cl:1][C:2]([Cl:11])=[CH:3][CH:4]([CH:8]([CH3:10])[CH3:9])[C:5](O)=[O:6].S(Cl)([Cl:14])=O>C1C=CC=CC=1>[Cl:1][C:2]([Cl:11])=[CH:3][CH:4]([CH:8]([CH3:10])[CH3:9])[C:5]([Cl:14])=[O:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24386Thionyl ChlorideHCID 13246126alpha-(2,2-Dichlorovinyl)isovaleric acid

生成物 1

HCID 20485210HCID 20485210、化合物

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

In 15 ml of dry benzene were dissolved 1.8 g of α-(2,2-dichlorovinyl)isovaleric acid, followed by the addition of 3.5 g of thionyl chloride. The mixture was refluxed for 5 hours and, then, distilled to remove the low-boiling fraction. By the above procedure there was obtained α-(2,2-dichlorovinyl)isovaleroyl chloride. This chloride was dissolved in 20 ml of benzene, and 2.0 g of α-ethynyl-3-phenoxybenzyl alcohol were added. This was followed by the addition of 2.9 g of pyridine and the mixture was stirred at room temperature for 8 hours. The resultant reaction mixture was diluted with diethyl ether, washed with water and dilute aqueous hydrogen chloride and dried over anhydrous magnesium sulfate. The low-boiling fraction was then distilled off and the residue was chromatographed on a column of silica gel (benzene/n-hexane=1:1 v/v). By the above procedure there were obtained 2.6 g of α-ethynyl-3-phenoxybenzyl α-(2,2-dichlorovinyl)isovalerate (compound [2]) having the following properties [yield: 71% based on α-(2,2-dichlorovinyl)isovaleric acid].

後処理

  1. temperatureThe mixture was refluxed for 5 hours
  2. distillationdistilled
  3. customto remove the low-boiling fraction

出典と根拠

ORDレコード
ord-861fd8182053465ca9ea262c1347f5de
出典データセット
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04409238

反応ノート

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